# FDA recall Z-1353-2021

> **Gf Health Products** · Class II · device recall initiated 2021-03-24.

## Product

Drop Arm Versamode"

## Reason for recall

The front casters on the 6810A Lumex Drop Arm Versamode are incorrect.

## Distribution

Distributed nationwide to CA, WI, PA, IL, and TX. Distributed internationally to Mexico and Canada.

## Key facts

- **Recall number:** Z-1353-2021
- **Recalling firm:** Gf Health Products
- **Classification:** Class II
- **Product type:** device
- **Status:** Terminated
- **Initiation date:** 2021-03-24
- **Report date:** 2021-04-14
- **Termination date:** 2023-05-01

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Atlanta, GA, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-1353-2021

## Citation

> AI Analytics. FDA recall Z-1353-2021. Retrieved 2026-06-24 from https://api.ai-analytics.org/recall/Z-1353-2021. Source: US FDA. Licensed CC0.

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